A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3620134



Internal ID7007007
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:27629744..27635092hg38UCSC Ensembl
Innerchr9:27629765..27635072hg38UCSC Ensembl
Outerchr9:27629724..27635113hg38UCSC Ensembl
chr9:27629742..27635090hg19UCSC Ensembl
Innerchr9:27629763..27635070hg19UCSC Ensembl
Outerchr9:27629722..27635111hg19UCSC Ensembl
Cytoband9p21.2
Allele length
AssemblyAllele length
hg385349
hg195349
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1462e214
Supporting Variantsessv13434740
SamplesHG00120
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3620134
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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